Canonical Allele Identifier: CA119997186

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71640816C>G , CM000667.2:g.71640816C>G	GRCh38
NC_000005.9:g.70936643C>G , CM000667.1:g.70936643C>G	GRCh37
NC_000005.8:g.70972399C>G	NCBI36
NG_008882.1:g.58529C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_022132.5:c.1000-187C>G MANE Select	NP_071415.1:n.1000-187C>G
ENST00000340941.11:c.1000-187C>G MANE Select	ENSP00000343657.6:n.1000-187C>G
NM_001363147.1:c.886-187C>G	NP_001350076.1:n.886-187C>G
NM_022132.4:c.1000-187C>G	NP_071415.1:n.1000-187C>G
ENST00000340941.10:c.1000-187C>G	ENSP00000343657.6:n.1000-187C>G
ENST00000505435.3:n.351-187C>G
ENST00000505435.4:n.956-187C>G
ENST00000505787.8:n.2904-3003C>G
ENST00000509358.6:c.1000-187C>G	ENSP00000420994.2:n.1000-187C>G
ENST00000509358.7:c.1064-187C>G	ENSP00000420994.3:n.1064-187C>G
ENST00000509539.2:c.389-3003C>G	ENSP00000425474.2:n.389-3003C>G
ENST00000509539.3:c.262-187C>G	ENSP00000425474.3:n.262-187C>G
ENST00000512218.6:c.886-187C>G	ENSP00000423202.2:n.886-187C>G
ENST00000629193.2:c.886-187C>G	ENSP00000486535.1:n.886-187C>G
ENST00000629193.3:c.886-187C>G	ENSP00000486535.2:n.886-187C>G
ENST00000681968.1:c.493-187C>G	ENSP00000508143.1:n.493-187C>G
ENST00000681991.1:n.1083+112C>G
ENST00000682045.1:c.856-187C>G	ENSP00000507329.1:n.856-187C>G
ENST00000682214.1:c.607-187C>G	ENSP00000507336.1:n.607-187C>G
ENST00000682231.1:n.18-187C>G
ENST00000682499.1:n.1821-187C>G
ENST00000682541.1:c.1000-3003C>G	ENSP00000507673.1:n.1000-3003C>G
ENST00000682667.1:n.1005C>G
ENST00000682687.1:c.1000-187C>G	ENSP00000507945.1:n.1000-187C>G
ENST00000682727.1:c.1064-3003C>G	ENSP00000507393.1:n.1064-3003C>G
ENST00000682876.1:c.1129-187C>G	ENSP00000508389.1:n.1129-187C>G
ENST00000683098.1:c.804-5395C>G	ENSP00000507670.1:n.804-5395C>G
ENST00000683258.1:c.*721-187C>G	ENSP00000507448.1:n.*721-187C>G
ENST00000683339.1:c.784-187C>G	ENSP00000507758.1:n.784-187C>G
ENST00000683403.1:c.910-187C>G	ENSP00000507896.1:n.910-187C>G
ENST00000683429.1:c.607-187C>G	ENSP00000507697.1:n.607-187C>G
ENST00000683665.1:c.1000-187C>G	ENSP00000507068.1:n.1000-187C>G
ENST00000683789.1:c.886-187C>G	ENSP00000507012.1:n.886-187C>G
ENST00000683847.1:n.1002-187C>G
ENST00000683882.1:c.1000-187C>G	ENSP00000506735.1:n.1000-187C>G
ENST00000684024.1:c.*671-187C>G	ENSP00000507175.1:n.*671-187C>G
ENST00000684254.1:c.*726-187C>G	ENSP00000508001.1:n.*726-187C>G
ENST00000684310.1:c.166-187C>G	ENSP00000507550.1:n.166-187C>G
ENST00000684474.1:n.401C>G
ENST00000684530.1:c.262-187C>G	ENSP00000507439.1:n.262-187C>G
ENST00000684686.1:n.432C>G
XM_005248567.1:c.886-187C>G	XP_005248624.1:n.886-187C>G
XM_011543528.1:c.1000-187C>G	XP_011541830.1:n.1000-187C>G
XM_017009688.1:c.1064-2955C>G	XP_016865177.1:n.1064-2955C>G
XR_001742172.1:n.1040-187C>G